Cyclopropylamine, 98+%
Cyclopropylamine, 98+%
Cyclopropylamine, 98+%
Thermo Scientific Chemicals

Cyclopropylamine, 98+%

CAS: 765-30-0 | C3H7N | 57.096 g/mol
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Catalog number A13844.30
also known as A13844-30
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544.65
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Quantity:
250 g
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Price (USD)
544.65
Online Exclusive
605.00
Save 60.35 (10%)
Each
Chemical Identifiers
CAS765-30-0
IUPAC Namecyclopropanamine
Molecular FormulaC3H7N
InChI KeyHTJDQJBWANPRPF-UHFFFAOYSA-N
SMILESNC1CC1
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SpecificationsSpecification SheetSpecification Sheet
Assay (GC)≥98.0%
Appearance (Color)Clear colorless to pale yellow
FormLiquid
Identification (FTIR)Conforms
Refractive Index1.4185-1.4225 @ 20?C
Cyclopropylamine) is used in the preparation of N-[4-(4-fluoro)phenyl-2-aminothiazol-5-yl]pyrimidin-2-yl-alkylamine derivatives. It is also used to prepare Pt(CPA)2(bismethylthiomethylenepropanedioate) and Pt(CPA)2(bisethylthiomethylenepropanedioate) complexes.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Cyclopropylamine) is used in the preparation of N-[4-(4-fluoro)phenyl-2-aminothiazol-5-yl]pyrimidin-2-yl-alkylamine derivatives. It is also used to prepare Pt(CPA)2(bismethylthiomethylenepropanedioate) and Pt(CPA)2(bisethylthiomethylenepropanedioate) complexes.

Solubility
Miscible with water, ethanol,ether and chloroform.

Notes
Hygroscopic. Incompatible with acids, acid chlorides, acid anhydrides, strong oxidizing agents and carbon dioxide.
RUO – Research Use Only

General References:

  1. Manakhov, A.; Nečas, D.; Čechal, J.; Pavliňák, D.; Eliáš, M.; Zajíčková, L. Deposition of stable amine coating onto polycaprolactone nanofibers by low pressure cyclopropylamine plasma polymerization. Thin Solid Films 2015, 581, 7-13.
  2. Miyamura, S.; Araki, M.; Suzuki, T.; Yamaguchi, J.; Itami, K. Stereodivergent Synthesis of Arylcyclopropylamines by Sequential C-H Borylation and Suzuki-Miyaura Coupling. Angew. Chem. Int. Ed. 2015, 54 (3), 846-851.